Miller syndrome   66038001

SNOMED CT code


SNOMED code66038001
nameMiller syndrome
statusactive
date introduced2002-01-31
fully specified name(s)Miller syndrome (disorder)
synonyms
  • Miller syndrome
  • Postaxial acrofacial dysostosis syndrome
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteLimb structure   66019005
Associated morphologyMorphologically abnormal structure   49755003
attributes - group3
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteFace structure   89545001
attributes - group2
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Finding siteBone structure   272673000
Associated morphologyDysplasia   25723000
parents
  • Skeletal dysplasia   105986008
  • Multiple malformation syndrome with facial-limb defects as major feature   23359005
  • Congenital anomaly of skeletal bone   8447006
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Disorder of skeletal system   88230002
          Skeletal dysplasia   105986008
            Miller syndrome   66038001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Disorder of limb   128605003
        Congenital anomaly of limb   60475009
          Multiple malformation syndrome with facial-limb defects as major feature   23359005
            Miller syndrome   66038001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Disorder of bone development   371521007
          Congenital anomaly of skeletal bone   8447006
            Miller syndrome   66038001

ancestors
sorted most to least specific
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